WO1998018882A1 - Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert-emulsionen - Google Patents
Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert-emulsionen Download PDFInfo
- Publication number
- WO1998018882A1 WO1998018882A1 PCT/EP1997/005798 EP9705798W WO9818882A1 WO 1998018882 A1 WO1998018882 A1 WO 1998018882A1 EP 9705798 W EP9705798 W EP 9705798W WO 9818882 A1 WO9818882 A1 WO 9818882A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- oil
- phase
- range
- pit
- temperature
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/26—Oil-in-water emulsions
- C09K8/28—Oil-in-water emulsions containing organic additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
- C09K8/36—Water-in-oil emulsions
Definitions
- the invention describes a method for facilitating the disposal of flowable and pumpable working materials based on emulsifiers containing W / O invert emulsions and for simplified cleaning of soiled solid surfaces by means of water-based rinsing aids.
- the elements of the action according to the invention on corresponding flowable and pumpable working materials for soil digestion - in particular corresponding borehole treatment agents - are shown, which, with the use of emulsifiers, have both an oil phase and an aqueous phase.
- treatment agents of this type the invention is described below with the aid of drilling fluids and drilling muds based thereon.
- auxiliary liquids of the type concerned here are, however, not restricted to this.
- Related fields of work affected by the invention are, for example, spotting fluids, spacers, packer fluids, auxiliary fluids for work over and stimulation and for fracturing.
- the use of the teaching according to the invention is of particular importance for the development of crude oil and natural gas, in particular in the offshore area, but is not restricted to this.
- the new teaching can also be used in general for land-based drilling, for example for geothermal drilling, water drilling, for performing geoscientific drilling and for drilling in the mining sector.
- liquid flushing systems for drilling rock holes while applying the detached cuttings are thickened, flowable systems that can be assigned to one of the following three classes:
- Closed oil-based drilling fluids are generally constructed as a three-phase system: oil, water and fine-particle solids.
- the aqueous phase is heterogeneously finely dispersed in the closed oil phase.
- additives are provided, in particular emulsifiers, weighting agents, fluid loss additives, alkali reserves, viscosity regulators, water-soluble salts and the like.
- emulsifiers for example, to the publication P.A. Boyd et al. "New Base Oil Used in Low-Toxicity Oil Muds” Journal of Petroleum Technology, 1985, 137 to 142 and R.B. Bennett “New Drilling Fluid Technology - Mineral Oil Mud” Journal of Petroleum Technology, 1984, 975 to 981 and the literature cited therein.
- Drilling fluids of the last described type and comparatively constructed other borehole treatment agents originally used mineral oil fractions as the oil phase. This is associated with a not inconsiderable impact on the environment if, for example, the drilling muds get into the environment directly or through the drilled rock.
- Mineral oils are difficult and practically not biodegradable and therefore can be regarded as long-term pollution.
- the experts involved have made a number of suggestions for exchanging the mineral oil fractions for more environmentally compatible and more easily degradable oil phases.
- the applicant describes possible alternatives for the oil phase in a larger number of property rights, and mixtures of such exchange oils can also be used.
- the broadest version of the invention is based on the task of disclosing a novel concept while maintaining and using the extensive technical knowledge existing today for the subject area according to the invention, which enables the desired optimization of the overall result.
- High technical performance should be accessible in an appropriate cost / benefit ratio and at the same time enable an optimized realization of the ecological requirements that exist today.
- This concept is formulated as a broad working principle which, using the specific specialist knowledge, varies in almost any number of specific embodiments and can thus be optimally adapted to the respective application.
- composition of the flowable and pumpable water and oil-based multicomponent mixture ensures that under specific conditions of use, particularly in the area of endangered rock formations within the borehole, the W / O invert flushing with the disperse aqueous phase is formed in the closed oil phase .
- the flowable working fluid is present as a W / O invert emulsion, which - in a known manner - on the rock surface provides the desired closure in the sense of Formation of a semipermeable membrane forms.
- the borehole stability can thus be achieved in an optimal form today.
- a targeted phase reversal to the O / W emulsion with a closed aqueous and disperse oil phase, however, at the same time now the facilities known to the experts in the processing and removal of the drilled and separated from the flushing phase separated cuttings .
- the dispersed form of the oil phase here can at least for the most part be easily rinsed off from the cuttings, whereby - depending on the ecological compatibility of the oil phase - a separate washing process or only simple dumping in seawater for offshore drilling can be provided .
- the disperse oil phase can be separated from the washing liquid or is accessible for easier aerobic degradation in the area of the sea water surface.
- the teaching according to the invention realizes this principle of phase inversion by utilizing a working parameter specified in the circular process of the drilling fluid, namely the temperature of the drilling fluid at the respective place of use. Temperatures within the borehole increase rapidly as the depth of the borehole increases. The heated drilling fluid phase, which is loaded with the hot cuttings, also leaves the borehole area at very high temperatures. By controlling and setting predetermined phase reversal temperatures, the desired reversal of the W / O invert phase to the O / W emulsion phase can now be specifically effected outside the borehole where such a phase reversal is desirable or even necessary for technical reasons.
- phase inversion according to the invention of the originally present W / O invert phase to the O / W emulsion phase opens up the decisive approach here. See the details below.
- the parameter of the phase inversion temperature (PIT) selected in the sense of the invention and thus predefined in the respective rinse ensures at the same time provides that the drilling fluid in the circuit has the desired state of the W / O invert emulsion in the drilling process on site.
- emulsifiers are compounds that combine hydrophilic and lipophilic building blocks in their molecular structure.
- HLB number value
- Emulsifiers or emulsifier systems with comparatively strongly hydrophilic components lead to high HLB values and, in their practical application, generally lead to water-based O / W emulsions with a disperse oil phase.
- Emulsifiers or emulsifier systems with comparatively strongly lipophilic fractions lead to comparatively lower HLB values and thus to the W / O invert emulsion with a closed oil phase and disperse water phase.
- the effect of the emulsifiers or emulsifier systems used can be influenced and thus changed by a plurality of accompanying factors in the overall mixture.
- Known parameters for these modifications in the context of the invention are, in particular: the loading of the aqueous phase with soluble organic and / or inorganic components, for example water-soluble, in particular polyhydric, lower alcohols and / or their oligomers, soluble inorganic and / or organic salts, that Quantity ratio of emulsifier / emulsifier system to the amount of oil and finally a constitutional vote in the structure of the emulsifier / emulsifier system on the one hand and the molecular structure of the oil phase on the other.
- soluble organic and / or inorganic components for example water-soluble, in particular polyhydric, lower alcohols and / or their oligomers, soluble inorganic and / or organic salts
- the respective temperature of the multicomponent system can be a parameter which is particularly meaningful in the sense of the teaching according to the invention for the emulsifier effect given in the specific case with regard to the formation of the O / W or the W / O emulsion state.
- at least partially nonionic emulsifiers / emulsifier systems show this effect of the pronounced temperature dependency in mixtures of oil and water phases which are not soluble in one another.
- phase inversion temperature PIT
- emulsifiers / emulsifier systems used lead to the following emulsion assignments:
- System temperatures below the PIT form the O / W emission state
- system temperatures above PIT form the W / O invert emulsion.
- the phase inversion of the system is brought about by shifting the temperature into the other temperature range.
- the W / O invert state with closed oil phase is guaranteed.
- the phase reversal of the flushing and thus the easier processing of parts to be separated off can be achieved in a simple manner.
- the heating that is always associated with the circulation of the drilling fluid in the interior of the earth ensures the desired high temperature range above the PIT of the system on the hot rock surface and thus its inerting against the dispersed water content of the drilling fluid at this location.
- phase equilibria of 3-component systems from aqueous phase / oil phase / surfactant in particular nonionic emulsifiers / emulsifier systems
- K. SHINODA and H. KUNIEDA Phase Properties of Emulsions: PIT and HLB" in " Encyclopedia of Emulsion Technology, 1983, Vol.1, 337 to 367.
- the authors include in their publication in particular also the relevant extensive printed prior art, in order to understand the teaching according to the invention given below in particular the knowledge of the temperature dependence of the phase inversion of such emulsifiers
- SHINODA describes the parameter of the phase inversion temperature (PIT, HLB temperature), the effect of the temperature dependence of the respective system using nonionic emulsifiers being particularly emphasized in the older publications by SHINODA et al. gem. Refs. 7 and 8.
- WINSOR I is the range of the stable water-based O / W phase
- WINSOR II corresponds to the range of the stable invert phase of the type W / O
- WINSOR III designates the middle phase and thus corresponds to the temperature range of the phase inversion PIT in the sense of current usage and the teaching according to the invention.
- phase inversion and the associated phase inversion temperature takes place within a temperature range, which in turn delimits itself with a lower limit against the O / W emulsion state and with its upper limit against the W / O invert emulsion state.
- the experimental testing of the respective system in particular by determining the conductivity at rising and / or falling temperature, gives measures for the respective lower and upper limits of PIT, whereby there may be slight shifts again if the conductivity test is in ascending temperature branch and on the other falling temperature branch can be determined.
- the phase inversion temperature (PIT) or rather the PIT range shows in this respect agreement with the definition of the previously explained WINSOR III (microemulsion) middle phase.
- the distance between the PIT lower limit (delimitation against O / W-) and the PIT upper limit (delimitation against W / O-Invert-) is usually a controllable temperature range that is comparatively limited by the choice of suitable emulsifier components or systems. Temperature ranges are frequently given here, which result in a difference value of less than 20 to 30 ° C., in particular not more than 10 to 15 ° C.
- the teaching according to the invention can make use of this if it wants to carry out the clear conversion of the invert flushing - or separated portions thereof - into the O / W emulsion state.
- the experimental determination of the conductivity of the system shows optimal conductivity in the area of water-based O / W flushing, in the area of the W / O invert phase there is generally no conductivity. If the conductivity is measured with temperature variation (increasing and / or decreasing) on an emulsion sample in the area of the phase inversion temperature, then the limit temperatures between the three areas named O / W-Mittelphase-W / O must be determined in a very precise manner. Regarding the conductivity or no longer existing conductivity of the two border areas, what has been said before applies; between these two areas lies the temperature section of the phase inversion of the respective system that occurs here, with its temperature limits down (conductivity given) and up (no conductivity) to be determined exactly is.
- the conductivity is determined on a multicomponent mixture which has first been heated to temperatures above the phase inversion temperature range and is then cooled in a predetermined manner.
- the upper and lower limit values for the phase inversion temperature range determined here do not have to be completely identical to the corresponding values of the previously described determination section with increasing temperature of the multi-component mixture.
- the respective limit values are stored so close to one another that large-scale work can be carried out using standardized parameters - in particular by averaging the limit values that belong to each other.
- the computational determination of the PIT of the respective multicomponent system can be expedient.
- this also applies to potential optimizations in the selection of the emulsifiers or emulsifier systems and their adaptation to the selection and mixing of the aqueous phase, on the one hand, and the type of the oil phase, on the other hand, as specified by other considerations regarding technical action.
- Relevant specialist knowledge has recently been developed from completely different fields, in particular from the field of cosmetics production. The invention provides for the use of this generally applicable specialist knowledge now and especially for the field of drilling of soil concerned according to the invention or for the treatment of already existing soil holes with systems containing oil and water phases.
- the aim of the invention is opposite to this step of tertiary oil production by flooding:
- the subject matter of the invention is, in a first embodiment, a method for facilitating the disposal of flowable and pumpable working materials based on W / O invert emulsions containing emulsifiers - in particular corresponding aids from the field of soil digestion, such as oil-based W / O invert drilling fluids - and for easier cleaning of soiled solid surfaces, if required, with the use of flowable flushing aids.
- This process according to the invention is characterized in that by selecting and matching the emulsifiers / emulsifier systems to the oil phase of the invert emulsion, a temperature-controlled phase inversion in the temperature range below the operating temperatures of the W / O invert emulsions is ensured, but at the same time this temperature-controlled Phase inversion takes place above the solidification of the aqueous phase by freezing.
- the invention is further characterized in that the disposal or cleaning is carried out in the temperature range of the phase inversion and / or at temperatures below.
- the cooling of the contaminated solid material or at least the cooling of the invert emulsion to be separated to the range of the phase inversion temperature (PIT) is ensured before and / or during the cleaning of the contaminated solid surfaces.
- PIT phase inversion temperature
- At least extensive separation of, in particular, coarse solids from portions of the material to be cleaned which are flowable and pumpable at working temperatures can be achieved under the influence of increased gravity.
- the soiled solid surfaces can be washed with water-based rinsing aids, in particular with cold water, the temperature of which is below the PIT range of the emulsion residues to be rinsed off. This washing process can be accelerated, in particular, by the introduction of mechanical energy, so that washing stages which are limited in time can be used. For details, see in the following.
- the teaching according to the invention relates in particular to the use of the method described here for facilitating cleaning and disposal of the cuttings from the earth borehole loaded with residual portions of the drilling mud during and / or preferably before its onshore or offshore -Deposition.
- Emulsifiers or emulsifier systems which are at least partly and preferably at least predominantly non-ionic in structure and / or combine both non-ionic structural elements and anionic structural elements in the basic molecular structure of the emulsifiers / emulsifier systems are particularly suitable for this purpose.
- nonionic emulsifiers / emulsifier systems can also be used as flowable components even at room temperature or only slightly elevated temperatures.
- the range of suitable nonionic emulsifiers is so broad and accessible from chemicals of both natural and synthetic origin that optimized emulsifier systems can be used from the point of view of ecological compatibility and in particular also of the marine toxicity that may have to be taken into account.
- the components essential here are accessible at low cost.
- nonionic emulsifier components are their pronounced temperature dependence of the PIT in the respective oil system, which can additionally be decisively controlled by the proportions in the mixture of the oil phase to the emulsifiers / emulsifier components - see the previously cited reference Förster et al.
- the emulsifiers / emulsifier systems are matched to the other parameters in the rinsing composition that are given in each case in such a way that the PIT of the multicomponent mixture is in a temperature range which, as a lower limit, is the cold washing of the solid surfaces to be cleaned with an aqueous phase allows.
- aqueous phase in the rinsing systems of the type in question, which contains considerable amounts of dissolved organic and / or inorganic auxiliaries, for example soluble salts for adjusting and regulating the pressure balance of the water phases competing with one another and their osmotic pressures in the surrounding rock of the earth well and on the other hand in the drilling fluid.
- auxiliaries for example soluble salts for adjusting and regulating the pressure balance of the water phases competing with one another and their osmotic pressures in the surrounding rock of the earth well and on the other hand in the drilling fluid.
- the solidification temperatures of such salt-laden aqueous phases can be significantly below 0 ° C - for example in the range from -10 to -20 ° C.
- a preferred lower limit for the PIT - or the PIT range - of the multicomponent mixture is, however, above 0 to 5 ° C and in particular for values in the range of 10 to 15 ° C or also at 20 ° C. The following explains the practical importance of these comparatively low limits for determining the PIT range down in connection with preferred specific embodiments for the action according to the invention.
- the upper limit of the temperature range for triggering the phase inversion should be at a sufficient distance from the range of the stable W / O invert emulsion.
- the upper limit of the temperature range mentioned for phase inversion is expediently at least 3 to 5 ° C. below the working temperature of the multi-component mixture in the area of the geological digestion. However, more pronounced distances between these two temperature parameters are preferred.
- the upper limit for the definition and determination of the PIT or the PIT range in the sense of the inventive action is at a maximum of 100 ° C. or only to a limited extent higher temperatures - for example at a maximum of 110 to 120 ° C.
- the upper limit for the selection and setting of the PIT is at temperatures below 100 ° C., for example at a maximum of approximately 80 to 90 ° C., preferably at a maximum of 60 ° C. and in particular in the temperature range up to a maximum of 50 ° C.
- multicomponent mixtures of the type specified may be particularly preferred, the PIT of which is within the temperature range from about 5 to 80 ° C., preferably in the range from about 10 to 60 ° C. and in particular in the temperature range from 15 to 50 ° C.
- numerical values for the PIT in the temperature range from 20 to 35 ° C. or also up to 40 ° C. can be particularly useful.
- the use of multi-component mixtures according to the invention for example as part of the drilling of the ground as a flowable and pumpable drilling fluid, provides for the continuous circulation of this liquid phase down into the ground and from there - loaded with the drilled cuttings - back up to the drilling platform.
- the drilled cuttings are - usually - separated and the recovered flowable and pumpable liquid phase is placed in a storage container, from which the invert mud is pumped down again into the borehole.
- the drilling fluid passes through a considerable temperature gradient within this cycle, even if the fluid loaded with cuttings is still conveyed hotly upwards.
- the technical stages of the screening and the intermediate storage of the rinsing phase in the storage container generally lead to a decrease in their own temperature, for example to values in the range from approximately 40 to 60 ° C.
- the teaching according to the invention provides a preferred embodiment in which the phase inversion does not occur in the flushing carried out in the circuit, even in the comparatively cooler areas outside the ground. If the PIT (the PIT range) of the system is set and maintained sufficiently below a predetermined limit value of, for example, 50 ° C., then this goal can be achieved with simple means. Even in cold seasons, such lower limit values for the temperature of the pumped-over invert sludge phase which is established in the circuit can be maintained in the rinsing circuit, for example by means of corresponding heating elements in the storage container.
- the advantages of the action according to the invention are now opening up:
- the PIT range is reached downwards and, if desired, the value falls short, so that the microemulsion agent phase initially occurs in the rinsing portions adhering to the cuttings and, with further temperature reduction, the phase Set water-based O / W emulsion phase. It immediately makes sense that the disposal of the residual oil adhering to the cuttings can be substantially simplified.
- drilling mud for land-based and / or preferably off-shore drilling of soil
- a PIT in the temperature range equal to / less than 50 ° C and, for example, with a PIT in the range from 20 to 35 ° C to use.
- the separated cuttings can now be subjected to a cleaning stage in a simplified manner - especially on site - or can also be disposed of by direct dumping.
- the optimal specific embodiment for this disposal step can be found. The following then applies in particular:
- the temperature-controlled inversion phase emulsion phase
- O / W emulsion state in these flushing residues quickly result from cooling in the seawater .
- the dilution effect of the surrounding sea water can have a full effect, the oil droplets formed no longer adhere to the rock and are therefore mobile. At least in part, they float upwards in the sea water, reach the area of comparatively increased oxygen concentrations in the aqueous phase and are there subject to the comparatively easier aerobic degradation.
- At least a partial cleaning of the cuttings to be disposed of from the oil phase can be carried out by a separate work step, preferably on site: when the temperature range for the inversion middle phase is set, the particularly easy wash-out sought in the prior art in the context of tertiary oil production is given the oil phase, so that, for example, a corresponding washing process can be carried out with water-based washing liquids, for example very simply sea water, without undue work.
- the range of O / W emulsion formation is set by further lowering the temperature.
- a separation into the aqueous phase and the oil phase as a potential work step of such a cleaning stage can thus be easily accomplished.
- the separation between flowable and pumpable parts - which remains of the drilling fluid - and the cuttings to be disposed of are substantially relieved. Different separation principles can be used separately or in combination with each other. Details of this are explained below.
- drilling muds preferred according to the invention for land-based and / or preferably for offshore drilling of soil, in particular for tapping oil and / or gas deposits can be designed in such a way that the drilling muds can be treated with a PIT in the temperature range equal to / less than 50 ° C, preferably equal to / less than 40 ° C and in particular in the range from 20 to 35 ° C.
- the PIT of the overall system can in particular be matched to the operating conditions of the drilling mud in such a way that the cuttings loaded with drilling mud after they have been separated from the main mass of the drilling mud by suitable separation processes, in particular using increased gravity and / or by washing with z.
- B. cold water - especially with sea water - and preferably with phase inversion W / O to O / W can be cleaned.
- the amount of oil on the cuttings to be disposed of can be reduced to such an extent that even in off-shore drilling, their disposal by simple dumping, even at high levels Requirements for the ecological compatibility of the drilling process in its entirety.
- the washing process can be carried out in one or more stages. As a rule, it will be preferred to work with washing stages which are limited in time, the duration of the respective washing stage being, for example, in the minute range, preferably at most about one minute or even significantly less.
- the respective properties of the items to be washed must be taken into account. It is obvious that when water-swellable clays are present in the cuttings to be cleaned, their willingness to swell while taking up water must be taken into account, while corresponding concerns with cuttings based on non-swellable minerals take a back seat.
- the teaching according to the invention provides for the combination of a plurality of working parameters to promote and facilitate the separation process between the solid phase on the one hand and the emulsion phase to be separated off on the other hand on the basis of the drilling mud residues.
- Combinations of washing stages and separation under the influence of increased effects of gravity are particularly considered here.
- the previously described separation of substances can be done by simply throwing off the soiled cuttings in the centrifuge at temperatures in the O / W emulsion range be reinforced that additional washing liquid is added to the items to be cleaned and in particular sprayed on.
- Water-based detergent and, in particular, very simply cold water are preferably used as cleaning aids. This washout aid can be applied once or in a plurality of successive stages to the solid material which is preferably kept in the centrifugal process.
- the improved cutting laundry with water-based rinsing aids is also possible without the use of centrifuge technology.
- General specialist knowledge enables the cold washing process to be optimized.
- the washing process can in principle be accelerated by introducing mechanical energy. It will generally be preferred to carry out the energy input into the aqueous detergent phase and accordingly to wash off the items to be cleaned in the sense of spray washing with raised pressures in one or more process stages.
- the subsequent washing stage according to the invention can thus be carried out, for example, directly on the solid material retained in a comparatively thin layer on the sieve.
- the appropriate pressure washing with application of the washing liquid by full-cone nozzle heads is particularly suitable, which can be designed in particular as corresponding pressure nozzles and, if desired, also as multi-component nozzles.
- a corresponding wash using multi-component nozzles from the field of air atomization is particularly effective.
- the nozzle set can be adjusted in a manner known per se by changing the air and liquid pressure so that either a particularly fine or coarse droplet atomization is achieved. This makes it possible to have a large control ratio of the amount of air to liquid while at the same time optimizing the energy input of the drop-shaped washing liquid and thus the rinsing result.
- the high-pressure washing can be carried out, for example, with pressures of the sprayed washing liquid phase from 2 to 200 bar, preferably from 10 to 100 bar.
- the distance between the nozzle jet and the solid surface to be cleaned is, for example, in the range of a maximum of 10 to 50 cm. Effective cleaning effects are achieved with limited amounts of washing liquid, which only make up a fraction of the cutting volume.
- the wash water containing the rinsed emulsion components can - if desired after an intermediate storage with partial phase separation - z. B. with a 3-phase separator - further separated in the water phase / oil phase and optionally a finely divided solid phase.
- a 3-phase separator further separated in the water phase / oil phase and optionally a finely divided solid phase.
- the extensive knowledge of the experts is available for the separation of appropriate water / oil emulsions or dispersions. It can work using purely mechanical equipment, especially by gravity separation in rapidly rotating centrifuges. Depending on the stability of the O / W mixtures present in the individual case, the use of appropriate separators with lower values for the gravitational number g can also be considered. In a manner known per se, both separators and centrifuges can be integrated into the separation process in a continuous process.
- washing liquids containing oil and water are known processes such as flotation or in particular also separation via membrane processes. If necessary, go through beforehand Addition of demulsifiers to an intense emulsion state in the washing liquid can be broken.
- oil phases or oil-mixed phases are suitable which are at least partially - preferably at least predominantly - assigned to the following classes of substances: Saturated hydrocarbons (straight-chain, branched and / or cyclic), olefinically unsaturated hydrocarbons, in particular of the type LAO (linear ⁇ -olefins), 10 (internal olefins) and / or PAO (polymeric ⁇ -olefins), aromatics, naphthenes, carboxylic acid esters, ethers , Acetals, carbonic acid esters, fatty alcohols, silicone oils, (oligos) amides, (oligo) imides and / or (oligo) ketones.
- Saturated hydrocarbons straight-chain, branched and / or cyclic
- olefinically unsaturated hydrocarbons in particular of the type LAO (linear ⁇ -olefins), 10 (internal olefins) and / or
- esters previously mentioned in this connection includes on the one hand corresponding esters of monocarboxylic acids and / or polycarboxylic acids, on the other hand corresponding esters of monofunctional alcohols and / or polyfunctional alcohols.
- esters of monocarboxylic acids and / or polycarboxylic acids on the other hand corresponding esters of monofunctional alcohols and / or polyfunctional alcohols.
- esters of polyfunctional alcohols with monocarboxylic acids and in particular glycerol esters of natural and / or synthetic origin can be used effectively as an oil phase or as a component of the oil phase for the first time. It has been known for years in relevant publications of the prior art that oils of natural origin - and thus corresponding glycerol-based triesters of higher unsaturated fatty acids - can be used as an ecologically compatible oil phase in W / O inverting.
- the teaching according to the invention also opens up the possibility of realizing the desired environmental protection to an extent not known to date.
- a work result which is still unknown to date can be set in terms of the objective of the invention.
- the possibility - known per se, but which can now be used with particular advantage according to the invention - of using selected mixtures of different oils as the oil phase of the rinsing system must also be taken into account.
- mixtures of comparatively heavy anaerobic and / or aerobically degradable oils with, on the other hand, particularly easily anaerobic and / or aerobically degradable oils can be used, which, in the form of cutting disposal optimized according to the invention, are an important step towards the goal of the invention Show overall optimization.
- a further possibility of modifying the W / O inverter system technology concerned here will be discussed first.
- W / O inverter systems of a conventional type and, in particular, corresponding invert drilling muds contain, according to current practice, the oil phase - based on the volume ratio of the sum of the oil and water phases - in an amount of at least 50% by volume.
- the content of the oil phase is usually significantly higher, for example in the range from 70 to 90% by volume of the oil / water mixture.
- the relevant literature also mentions oil-depleted invert rinsing, but in practice, in particular the systems required today with adequate ecological compatibility, this area of comparatively low-oil blends does not play a role.
- the range of the phase inversion temperature is determined, among other things, by the quantitative ratio of the oil phase to, in particular, the nonionic emulsifier / emulsifier system.
- the stability of the W / O invert emulsion in practical work is increased so much that the range for practically usable quantitative ratios in the respective oil / water mixture is substantially expanded.
- proportions (parts by volume) of the water-based phase (W) to the oil phase (oil) in the following ranges are accessible for the construction of the multiphase and preferably pumpable mixtures: 90 to 10 W to 10 to 90 oil.
- Mixing ratios of 85 to 20 W to 15 to 80 oil can be preferred.
- W / oil mixing ratios it is possible to work with W / oil mixing ratios without difficulty, which the W phase in quantities of at least 30 or 40 parts by volume or even at least 50 parts by volume - and for example in quantities of 55 to 85 parts by volume - included.
- the oil phase can thus also become a subordinate component, for example in the range from at least 10 to 15 parts by volume, preferably from 20 to 50 parts by volume. Because of the sum of W and oil - stable W / O invert conditions in the temperature range of practical use inside the soil are guaranteed. In this sense, multicomponent mixtures may be preferred according to the invention, the proportion of water-based phase (% by volume based on mixture W / oil) equal to / greater than 30 to 35%, preferably equal to / greater than 40% and further preferably equal to / greater than 50% , is.
- the mixing range with a predominant proportion of water can be of particular importance, with amounts of up to 85% by volume and in particular the range from 55 or 60 to 80% by volume of the water-based phase again being particularly preferred.
- W / O inverter rinses with a heavily emaciated oil phase content, which - based on the liquid phases - must not make up more than 20 to 40% by volume but nevertheless meet the requirements in use, fall within the scope of the invention. It is immediately evident that disposal is also made considerably easier here.
- phase inversion temperature for given substance mixtures from oil phase, emulsifier or emulsifier mixtures and can be used using the specialist knowledge also cited at the beginning (SHINODA et al. And Th. Förster et al.) aqueous phase can be calculated. Accordingly, some additional determination elements preferred according to the invention for the selection of the emulsifiers or emulsifier systems are introduced below.
- phase inversion temperature PIT
- Components with corresponding HLB values in the range from about 6 to 20 and preferably from 7 to 18 have proven to be suitable nonionic main emulsifier components. These main components are preferably used together with more lipophilic co-emulsifiers, which - based on the respective main emulsifier component (s) - in turn have lower HLB (number) values. Accordingly, useful co-emulsifiers are initially in the number range below the previously mentioned number range for the main emulsifier component (s). Suitable co-emulsifiers can also fall within this range of numbers with their HLB value, but are then generally lower than the main emulsifier component ⁇ ) present in a mixture with their respective individual numerical values.
- the W / O emulsifiers used today in the practical process, in particular in oil-based invert rinses, can be used in an important embodiment of the inventive Teaching take over the function of the comparatively more lipophilic co-emulsifier in the emulsifier mixtures defined according to the invention.
- W / O emulsifiers in oil-based inverting rinses which are in industrial use today are compounds from the class of anionically modified oligo-aminoamides of long-chain fatty acids.
- the calcium salts of these components which form in the presence of lime (lime) have pronounced W / O emulsifier action.
- particularly suitable main emulsifier components and / or co-emulsifiers can be assigned to at least one of the following classes of substances from the large range of nonionic emulsifiers:
- alkoxylates in particular low alkoxylates, in which case corresponding ethoxylates and / or propoxylates are of particular importance - of base molecules containing lipophilic residues and capable of alkoxylation of natural and / or synthetic origin.
- the length of the alkoxylate residues in relation to the lipophilic residues present in the molecule determines the respective mixing ratio of hydrophilic and hydrophobic behavior and the associated assignment of the HLB values.
- alkoxylates of the stated type are known as such - i.e. with a free hydroxyl group at the alkoxylate residue - nonionic emulsifiers, but the corresponding compounds can also be end group-sealed, for example by esterification and / or etherification.
- nonionic emulsifiers for the purposes of the invention are partial esters and / or partial ethers of polyfunctional alcohols with in particular 2 to 6 C atoms and 2 to 6 OH groups and / or their oligomers with acids and / or alcohols containing lipophilic radicals.
- Compounds of this type are also particularly suitable which additionally contain (oligo) alkoxy radicals and, in particular, corresponding oligo-ethoxy radicals integrated into their molecular structure.
- the polyfunctional alcohols with 2 to 6 OH groups in the base molecule or the oligomers derived therefrom can in particular be diols and / or triols or their oligomerization products, the glycol and the glycerol or their oligomers being particularly important.
- other polyfunctional alcohols of the type summarized here such as trimethylolpropane, pentaerythritol and glycosides - or their respective oligomers - can also be basic molecules for the reaction with acids and / or alcohols containing lipophilic residues, which are then important emulsifier components in the sense of the invention are.
- Known nonionic emulsifiers of the ethylene oxide / propylene oxide / butylene oxide block polymer type can also be assigned to the area of partial ethers of polyfunctional alcohols.
- emulsifier components are alkyl (poly) glycosides of long-chain alcohols and the already mentioned fatty alcohols of natural and / or synthetic origin or alkylolamides, amine oxides and lecithins.
- APG compounds alkyl (poly) glycoside compounds
- emulsifier components can include be particularly interesting because it is an emulsifier class with particularly good ecological compatibility. It is e.g. to control the phase inversion into the temperature ranges described according to the invention, it is also possible, in part, to use other main emulsifier components, e.g. Nonionic surfactant compounds with more pronounced phase inversion behavior can also be used.
- the oligo alkoxylate compounds already mentioned several times, in particular corresponding compounds of the oligo ethoxylate component type.
- the (oligo) alkoxylates of basic molecules containing lipophilic residues can in particular be derived from selected representatives from the following classes of basic molecules containing lipophilic residues: fatty alcohols, fatty acids, Fatty amines, fatty amides, fatty acid and / or fatty alcohol esters and / or ethers, alkanolamides, alkylphenols and / or their reaction products with formaldehyde and further reaction products of carrier molecules containing lipophilic residues with lower alkoxides. As indicated, the respective reaction products can also be at least partially end group-sealed.
- partial esters and / or partial ethers of polyfunctional alcohols are in particular the corresponding partial esters with fatty acids, for example of the type of glycerol monoesters and / or diesters, glycol monoesters, corresponding partial esters of oligomerized polyfunctional alcohols, sorbitan partial esters and the like, and corresponding compounds with ether groups. You can refer to the extensive specialist knowledge here.
- Such partial esters and / or ethers can in particular also be basic molecules for an (oligo) alkoxylation.
- an essential determining element for the teaching according to the invention is that the quantity of emulsifiers / emulsifier systems used in the multicomponent mixture is matched to the proportion of oil phase present here. Accordingly, preferred amounts of emulsifier are in the range equal to or greater than 1% by weight, preferably in the range from 5 to 60% by weight, based in each case on the oil phase.
- the following quantitative ranges for the emulsifiers / emulsifier systems used according to the invention - again based on the oil phase - have proven to be particularly suitable for practical work: 10 to 50% by weight, advantageously 15 to 40% by weight and in particular amounts in the range from 20 to 35% by weight.
- the - initially emulsifier-free - oil phase is said to be at least predominantly insoluble in the aqueous emulsion phase and is preferably flowable and pumpable even at room temperature. Flash points of the oil phases above 50 to 60 ° C, preferably equal / greater 80 to 100 ° C and in particular equal to or greater than 120 ° C are desirable or preferred. It may also be expedient to use oil phases which have a Brookfield (RVT) viscosity of not more than 55 mPas and preferably not more than 45 mPas in the temperature range from 0 to 10 ° C.
- RVT Brookfield
- the mixtures of aqueous phase, oil phase, emulsifiers and conventional additives which are designed as drilling mud.
- the mixture formed as drilling mud in the temperature range from 10 to 15 ° C. above the limit temperature between the emulsion medium phase and the W / O invert range has a plastic viscosity (PV) not greater than 100 mPas.
- PV plastic viscosity
- Corresponding drilling muds are preferred, the PV value of which is not greater than 80 mPas and in particular in the range from 30 to 45 mPas.
- the flow limit (YP) of drilling muds constructed according to the invention should not be greater than 80 lb / 100 ft 2 in the temperature range from 10 to 15 ° C.
- this yield point here are values not greater than 50 lb / 100 ft 2 and in particular in the range above 4 to 5 lb / 100 ft 2 , for example in the range from 10 to 25 lb / 100 ft 2 .
- water-based emulsion rinses and in particular rinsing systems of the O / W type can also be stabilized against the undesired settling of dispersed solids in the rinsing by using water-soluble polymer compounds, even in the comparatively low temperature range.
- Suitable water-soluble polymer compounds of both natural and synthetic origin are basically suitable here. The relevant specialist knowledge can be referred to here.
- the teaching according to the invention provides for the possibility, if necessary, of cooling the drilling fluid as a whole outside the area of use to such an extent that the phase inversion to the O / W emulsion flushing takes place here.
- the rules applicable in this field of work then apply to the sufficient stabilization of the system, so that the use of such stabilizing water-soluble polymer compounds and / or water-swellable clays can also be considered. Their presence in the state of the W / O inverter flushing in the hot work area does not disturb.
- a characteristic feature of all auxiliary fluids and in particular drilling fluids in the sense of the definition according to the invention remains despite the use of all auxiliary substances known per se: the correct selection and coordination of the emulsifiers / emulsifier systems in terms of type and quantity, in particular the nature of the oil phase used, forms in contact with the W / O invert phase above the emulsion medium phase from the inside of the soil and the high working temperature that arises here, at least at the contact surface of hot soil / emulsion. Outside of the working area in the interior of the ground, the temperature is reduced, and again the selection and coordination of the parameters mentioned above can control the behavior of the parts of the drilling fluid located here, in their entirety or in parts separated again therefrom, in a wide variety of ways.
- the objective of the invention formulated at the outset can thus be achieved in a previously unknown manner.
- Example 1 to 7 first compile frame formulations which are characterized by the basic system oil phase / water or aqueous phase / emulsifier or emulsifier system. While the recipe of Example 1 is limited to these basic components, in the following Examples 2 to 7, customary additional components from the field of drilling muds are also used.
- the respective numerical values for the temperature range of the phase inversion - PIT / ° C - are assigned to the respective system.
- the PIT range is characterized by its lower and upper temperature limits.
- phase inversion temperature is determined experimentally by determining the electrical conductivity of the aqueous emulsions as a function of the temperature. Details of the test procedure can be found in the publications EP 0 345 586 and EP 0 521 981 already named in the general description section.
- OMC 586 oil phase based on an ester mixture of essentially saturated fatty acids based on palm kernel and 2-ethylhexanol, which largely derives from C 12/14 fatty acids
- Emulsifiers are:
- HEC Hydroxyethyl cellulose
- Ratio of oil phase / aqueous phase (5% CaCl 2 ) in equal amounts by weight
- the proportion of the oil phase is greatly leaned compared to the aqueous phase (12 parts by weight to 41 parts by weight of the aqueous phase). No thickener soluble in cold water is used in the recipe.
- Example 2b The basic formulation of Example 2b is retained, but with the following
- the salt content of the aqueous phase is 5% by weight of CaCl 2 - 41 -
- the temperature range of the phase inversion (PIT / ° C) is determined on all substance mixtures.
- the viscosity of the substance mixtures is determined at a temperature significantly below the PIT range - viscosity at 25 ° C - and on the other hand at a temperature significantly above the PIT range - viscosity at 70 ° C.
- Example 2 c The clear reduction in the PIT range by increasing the salt concentration in the aqueous phase is also evident here (Example 2 c compared to Example 2 b).
- the low viscosity of the multicomponent mixture in the state of the water-based O / W rinse at temperatures below the PIT (Example 2 b) is compensated for by the use of the small amount of polymeric thickener based on HEC.
- Examples 3a and 3b below modify the oil phase of the respective multicomponent mixture.
- the ester oil OMC 586 is now used. In doing so - based on the basic recipes of Example 2 - the oil phase and the water phase are used in equal quantities (Example 3 a) and subsequently (Example 3 b) the O / W ratio is again very thin.
- the temperature range of the phase inversion is determined for both substance mixtures.
- Example 3b Based on the recipe of Example 3b, an ester oil-based rinse is put together and the temperature range of the phase inversion is determined.
- the two measured range values in the ascending temperature branch (PIT / ° C "upwards") and in the descending temperature branch (PIT / ° C "downwards") are listed separately.
- Example 5 a Based on the approaches of Example 3 - with the same emulsifier - two rinsing approaches are compared with one another, which contain the oil phase / water phase in a ratio of 1: 1 (Example 5 a), and on the other hand have the oil phase in a strongly emaciated ratio.
- the specific temperature ranges for the phase inversion - PIT / ° C ("upwards") and PIT / ° C ("downwards”) - are assigned to the respective recipe approaches in the table below. 45 -
- the emulsifier system is changed while maintaining the oil phase from example 5.
- An emulsifier combination of a comparatively hydrophilic polyol fatty acid ester Cetiol HE is used here, which is used in combination with a more hydrophobic co-emulsifier (Dehymuls SML).
- Examples 6 a and 6 b work with batches of the oil phase / aqueous salt phase of 1: 1 and otherwise identical amounts of additives, but change the mixing ratio of the two components of the emulsifier combination.
- the comparison of the respectively determined temperature ranges for the phase inversion - PIT / ° C ("upwards") and PIT / X (“downwards") - shows that by varying the quantity ratios of the emulsifier components to one another, a clear control of the PIT ranges which arise in each case becomes possible.
- Example 6 c varies - in the sense of the previous examples - again the oil / water ratio in the approach towards a comparatively low-oil mixture of substances, but here too the W / O inversion range required in practical use is not guaranteed only in the hot bore, but also in comparatively cooler outside areas of the circulation of the drilling fluid.
- a rinsing system is chosen with equal proportions of oil phase and aqueous 30% by weight calcium chloride solution - Example 7 a -, while in the second case the weight ratio of the water phase to the oil phase is about 2: 1.
- Example 7 b with its temperature range of phase inversion from about 20 to At 25 ° C, a number of drilling fluid systems based on oil phases known today are being put together for the field of W / O invert drilling fluids. Then the viscosity parameters are determined as follows on the unaged and on the aged material:
- the aging of the respective drilling fluid according to The standard recipe from Example 7b is made by treatment for 16 h at 250 ° F in an autoclave - in a roller oven.
- the multi-component mixtures tested correspond to the following recipe:
- rapeseed oil is used as a triglyceride of natural origin.
- the key figures determined for the unaged and aged material are listed in the table below. 49
- the di-n-octyl ether Cetiol OE is used as the oil phase.
- the characteristic values determined on the unaged and on the aged material are as follows:
- Isotridecyl alcohol is now used as the closed oil phase.
- the values determined on the system are as follows:
- the oil phase used here is the commercial product XP07 from Baroid, a flowable oil phase based on saturated paraffins.
- ester oil OMC 586 is used here as the oil phase.
- the following key figures are determined on the unaged and the aged rinse: 51 -
- This co-emulsifier is combined with different main emulsifier components in the sense of the definition according to the invention.
- the following oil phases - each together with 30% by weight aqueous calcium chloride solution - are used:
- Example 10 a Mineral oil Ha-359
- the oil / water ratios (vol.%) Used are varied in 5 test batches.
- the following oil / water mixing ratios are used: 40/60; 50/50; 60/40; 70/30; 80/20.
- a mixture of Lutensol TO5 as the main emuigator component and Ez-Mul NTE as the co-emulsifier is used as an emulsifier system in all batches.
- the following table first summarizes the quantitative proportions of the 5 blends tested in the test batch.
- the rheological values of plastic viscosity (PV in mPas), yield point (YP in lb / 100 ft 2 ) and gel strength (gel 10710 'in lb / are then measured on these multicomponent mixtures before aging (BHR) and after aging (AHR). 100 ft 2 ).
- the respective drilling fluid is aged in a conventional manner at 250 ° F for 16 hours in the roller-oven.
- the viscosity data is also determined in a conventional manner, see the details of Example 8 in this regard.
- the table below shows test series within the meaning of the invention using emulsifier systems which use APG compounds as a component of the main emulsifier component) or as the sole main emulsifier component.
- APG component comes the C 12 marketed by the applicant under the trade name APG 600. 16 APG product for use.
- the W / O invert emulsifier Ez-Mul NTE is also a co-emulsifier.
- the following table shows the composition of the drilling fluid emulsions in% by weight, as well as the temperature ranges (PIT / ° C upwards) for the phase inversion.
- Example 13a uses beet oil as the sole component of the oil phase.
- Example 13b uses a blend of 1 part by weight of rapeseed oil and slightly more than 4 parts by weight of OMC 586 ester oil as the oil phase.
- the respective weight composition (in g) of the two emulsion batches tested can be found in the table below. According to the information in Example 8, both drilling fluid emulsions are aged at 250 ° F for a period of 16 hours and then examined at 50 ° C in the manner described in Example 8 for their essential rheological data. The numerical values found before aging (BHR) and after aging (AHR) are assigned to the respective rinsing batches in the table below.
- the PIT temperatures determined are assigned to the non-aged and the aged rinsing batches.
- the temperatures at which the conductivity reaches 0 mS / cm are given as numerical values.
- solids are wetted with invert drilling fluid systems and then treated in a centrifuge.
- the cuttings are then placed on a sieve; Allow to drip for 1 minute with occasional shaking and then weigh the oil-laden cuttings to determine the amount of drilling fluid adhering.
- the cuttings are then transferred to a centrifuge tube, located cm high is on the bottom 2 cotton wool to absorb centrifuged to rinse, and 1, centrifuged for 5 minutes at 1800 min '1.
- hydrophobic constituents primarily esters and possibly emulsifiers
- the methylene chloride fraction is evaporated.
- the hydrophobic components remain in the residue.
- the amount of extracted hydrophobic constituents was 10% by weight (based on the amount of the rinse originally adhering to the cuttings), but only 5% by weight in the case of the rinse 14b.
- Drilling mud A normal invert mud
- Drilling fluid B (drilling fluid with PIT at 40 ° C):
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Earth Drilling (AREA)
- Processing Of Solid Wastes (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
Description
Claims
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97948769A EP0951519B1 (de) | 1996-10-30 | 1997-10-21 | Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert-emulsionen |
AT97948769T ATE211162T1 (de) | 1996-10-30 | 1997-10-21 | Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert- emulsionen |
AU69087/98A AU726703B2 (en) | 1996-10-30 | 1997-10-21 | A process for the simplified disposal of working fluids based on w/o invert emulsions |
UA99052948A UA54468C2 (uk) | 1996-10-30 | 1997-10-21 | Спосіб полегшення утилізації робочих засобів на основі водно-масляних інвертних емульсій |
BR9712459-1A BR9712459A (pt) | 1996-10-30 | 1997-10-21 | Processo para o descarte simplificado de fluidos de lavra à base de emulsões invertida |
US09/297,481 US6165946A (en) | 1996-10-30 | 1997-10-21 | Process for the facilitated waste disposal of working substances based on water-in-oil invert emulsions |
DE59705924T DE59705924D1 (de) | 1996-10-30 | 1997-10-21 | Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert-emulsionen |
NZ335491A NZ335491A (en) | 1996-10-30 | 1997-10-21 | Process for the facilitated waste disposal of working substances based on water-in-oil invert emulsions |
JP10520005A JP2001502749A (ja) | 1996-10-30 | 1997-10-21 | w/o型インバートエマルジョンをベースとする作業液の容易な廃棄処理法 |
DK97948769T DK0951519T3 (da) | 1996-10-30 | 1997-10-21 | Fremgangsmåde til lettet bortskaffelse af arbejdsmidler på basis af V/O-invert-emulsioner |
CA002271040A CA2271040A1 (en) | 1996-10-30 | 1997-10-21 | A process for the simplified disposal of working fluids based on w/o invert emulsions |
NO992077A NO992077L (no) | 1996-10-30 | 1999-04-29 | FremgangsmÕte for forenklet avfallsivaretagelse av arbeidsmidler basert pÕ vann-i-olje-invertemulsjoner |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19643840.3 | 1996-10-30 | ||
DE19643840A DE19643840A1 (de) | 1996-10-30 | 1996-10-30 | Verbesserte Mehrkomponentengemische für den Erdreichaufschluß |
DE1997133710 DE19733710A1 (de) | 1997-08-04 | 1997-08-04 | Verfahren zur erleichterten Entsorgung von Arbeitsmitteln auf Basis von W/O-Invert-Emulsionen |
DE19733710.4 | 1997-08-04 | ||
US08/933,188 US6022833A (en) | 1996-10-30 | 1997-09-18 | Multicomponent mixtures for use in geological exploration |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998018882A1 true WO1998018882A1 (de) | 1998-05-07 |
Family
ID=27216768
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1997/005798 WO1998018882A1 (de) | 1996-10-30 | 1997-10-21 | Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert-emulsionen |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0951519B1 (de) |
CN (1) | CN1235627A (de) |
AU (1) | AU726703B2 (de) |
BR (1) | BR9712459A (de) |
NO (1) | NO992077L (de) |
WO (1) | WO1998018882A1 (de) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1103697A1 (de) * | 1999-11-26 | 2001-05-30 | ENI S.p.A. | Verfahren zur Verminderung des Polymeradsorption von Gesteinenmatrix |
EP1103589A1 (de) * | 1999-11-26 | 2001-05-30 | ENI S.p.A. | Bohrflüssigkeiten enthaltend Öl-in -Wasser Emulsionen |
US7008907B2 (en) | 2001-10-31 | 2006-03-07 | Halliburton Energy Services, Inc. | Additive for oil-based drilling fluids |
US7271132B2 (en) | 2001-10-31 | 2007-09-18 | Halliburton Energy Services, Inc. | Metallic soaps of modified fatty acids and rosin acids and methods of making and using same |
CN102003159A (zh) * | 2010-11-18 | 2011-04-06 | 四机赛瓦石油钻采设备有限公司 | 固井水泥混浆作业的自动控制方法 |
CN103540299A (zh) * | 2012-07-12 | 2014-01-29 | 中国石油化工股份有限公司 | 用于低压水敏地层的钻井液 |
WO2021048578A1 (en) * | 2019-09-09 | 2021-03-18 | Total Se | Method for determining the formation of a winsor iii microemulsion system |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100404638C (zh) * | 2006-07-07 | 2008-07-23 | 中国石油天然气股份有限公司 | 高密度压裂液 |
DE102007021795A1 (de) | 2007-05-07 | 2008-11-13 | Henkel Ag & Co. Kgaa | Textilbeduftung |
EA201301026A1 (ru) * | 2011-04-13 | 2014-08-29 | Мэн Ойл Груп Аг | Концентрат на основе эмульгаторов и его применение для обработки загрязнений нефтяными продуктами |
CN103059829B (zh) * | 2013-01-25 | 2014-08-20 | 中国石油大学(华东) | 一种致密气藏气井用纳米乳液型控水压裂液及其制备方法 |
CN107922821A (zh) * | 2015-08-07 | 2018-04-17 | 艺康美国股份有限公司 | 用于油包水胶乳的非离子转化剂和使用方法 |
CN109401745B (zh) * | 2018-11-21 | 2021-03-12 | 西南石油大学 | 一种自适应流度控制体系及其在高温高盐油藏的应用 |
CN112574351A (zh) * | 2020-12-08 | 2021-03-30 | 爱森(中国)絮凝剂有限公司 | 一种速溶高渗透阴离子聚丙烯酰胺印染增稠剂的制备方法 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0047370A1 (de) * | 1980-09-10 | 1982-03-17 | Hüls Aktiengesellschaft | Verfahren zur Gewinnung von Öl aus einer unterirdischen Lagerstätte |
EP0117970A2 (de) * | 1983-03-04 | 1984-09-12 | Hüls Aktiengesellschaft | Verfahren zur Gewinnung von Öl aus Speichergestein |
EP0213321A2 (de) * | 1985-08-31 | 1987-03-11 | Hüls Aktiengesellschaft | Verfahren zur Injektivitätserhöhung von Einpressbohrungen bei der Ölförderung mittels Wasserfluten |
DE3819193A1 (de) * | 1988-06-06 | 1989-12-07 | Henkel Kgaa | Verfahren zur herstellung stabiler, niedrigviskoser oel-in-wasser-emulsionen polarer oelkomponenten |
WO1992002594A1 (de) * | 1990-08-03 | 1992-02-20 | Henkel Kommanditgesellschaft Auf Aktien | Verwendung oberflächenaktiver alkylglycosidverbindungen in wasser- und öl-basierten bohrspülungen und anderen bohrlochbehandlungsmitteln |
WO1992013926A1 (de) * | 1991-01-31 | 1992-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Verwendung oberflächenaktiver carbonsäure-komplexester als emulgatoren in öl-basierten bohrspülungen und anderen bohrlochbehandlungsmitteln |
WO1993016145A1 (en) * | 1992-02-12 | 1993-08-19 | Exxon Chemical Patents Inc. | Functional fluid |
-
1997
- 1997-10-21 WO PCT/EP1997/005798 patent/WO1998018882A1/de active IP Right Grant
- 1997-10-21 AU AU69087/98A patent/AU726703B2/en not_active Ceased
- 1997-10-21 EP EP97948769A patent/EP0951519B1/de not_active Expired - Lifetime
- 1997-10-21 CN CN97199205.3A patent/CN1235627A/zh active Pending
- 1997-10-21 BR BR9712459-1A patent/BR9712459A/pt not_active Application Discontinuation
-
1999
- 1999-04-29 NO NO992077A patent/NO992077L/no not_active Application Discontinuation
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0047370A1 (de) * | 1980-09-10 | 1982-03-17 | Hüls Aktiengesellschaft | Verfahren zur Gewinnung von Öl aus einer unterirdischen Lagerstätte |
EP0117970A2 (de) * | 1983-03-04 | 1984-09-12 | Hüls Aktiengesellschaft | Verfahren zur Gewinnung von Öl aus Speichergestein |
EP0213321A2 (de) * | 1985-08-31 | 1987-03-11 | Hüls Aktiengesellschaft | Verfahren zur Injektivitätserhöhung von Einpressbohrungen bei der Ölförderung mittels Wasserfluten |
DE3819193A1 (de) * | 1988-06-06 | 1989-12-07 | Henkel Kgaa | Verfahren zur herstellung stabiler, niedrigviskoser oel-in-wasser-emulsionen polarer oelkomponenten |
WO1992002594A1 (de) * | 1990-08-03 | 1992-02-20 | Henkel Kommanditgesellschaft Auf Aktien | Verwendung oberflächenaktiver alkylglycosidverbindungen in wasser- und öl-basierten bohrspülungen und anderen bohrlochbehandlungsmitteln |
WO1992013926A1 (de) * | 1991-01-31 | 1992-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Verwendung oberflächenaktiver carbonsäure-komplexester als emulgatoren in öl-basierten bohrspülungen und anderen bohrlochbehandlungsmitteln |
WO1993016145A1 (en) * | 1992-02-12 | 1993-08-19 | Exxon Chemical Patents Inc. | Functional fluid |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1103697A1 (de) * | 1999-11-26 | 2001-05-30 | ENI S.p.A. | Verfahren zur Verminderung des Polymeradsorption von Gesteinenmatrix |
EP1103589A1 (de) * | 1999-11-26 | 2001-05-30 | ENI S.p.A. | Bohrflüssigkeiten enthaltend Öl-in -Wasser Emulsionen |
US6499539B1 (en) | 1999-11-26 | 2002-12-31 | Eni S.P.A. | Process for reducing the adsorption of polymers onto rock matrix |
US6632777B1 (en) | 1999-11-26 | 2003-10-14 | Eni S.P.A. | Drilling fluids comprising oil emulsions in water |
US7008907B2 (en) | 2001-10-31 | 2006-03-07 | Halliburton Energy Services, Inc. | Additive for oil-based drilling fluids |
US7271132B2 (en) | 2001-10-31 | 2007-09-18 | Halliburton Energy Services, Inc. | Metallic soaps of modified fatty acids and rosin acids and methods of making and using same |
CN102003159A (zh) * | 2010-11-18 | 2011-04-06 | 四机赛瓦石油钻采设备有限公司 | 固井水泥混浆作业的自动控制方法 |
CN103540299A (zh) * | 2012-07-12 | 2014-01-29 | 中国石油化工股份有限公司 | 用于低压水敏地层的钻井液 |
CN103540299B (zh) * | 2012-07-12 | 2017-04-12 | 中国石油化工股份有限公司 | 用于低压水敏地层的钻井液 |
WO2021048578A1 (en) * | 2019-09-09 | 2021-03-18 | Total Se | Method for determining the formation of a winsor iii microemulsion system |
Also Published As
Publication number | Publication date |
---|---|
BR9712459A (pt) | 1999-10-19 |
AU726703B2 (en) | 2000-11-16 |
CN1235627A (zh) | 1999-11-17 |
NO992077D0 (no) | 1999-04-29 |
EP0951519A1 (de) | 1999-10-27 |
NO992077L (no) | 1999-04-29 |
EP0951519B1 (de) | 2001-12-19 |
AU6908798A (en) | 1998-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2411483B1 (de) | Emulsionsbasierte reinigungszusammensetzung für ölfeldanwendungen | |
EP0386636B2 (de) | Ester von Carbonsäuren mittlerer Kettenlänge als Bestandteil der Ölphase in Invert-Bohrspuelschlämmen | |
DE69408167T2 (de) | Lösungsmittelseifen und verfahren zur verwendung derselben | |
US6165946A (en) | Process for the facilitated waste disposal of working substances based on water-in-oil invert emulsions | |
DE3237630C2 (de) | ||
EP1546282B1 (de) | Bohrlochbehandlungsmittel mit niedrig-toxischer ölphase | |
EP0951519B1 (de) | Verfahren zur erleichterten entsorgung von arbeitsmitteln auf basis von w/o-invert-emulsionen | |
EP2201083B1 (de) | Verdicker für ölbasierte bohrspülmittel | |
EP0532570A1 (de) | Fliessfähige bohrlochbehandlungsmittel auf basis von kohlensäurediestern. | |
EP0765368A1 (de) | Lineare alpha-olefine enthaltende fliessfähige bohrlochbehandlungsmittel, insbesondere entsprechende bohrspülungen | |
WO1993013882A1 (de) | Verbesserte entsorgung von kontaminiertem bohrklein | |
EP1020507B1 (de) | Verbesserte Mehrkomponentengemische für den Erdreichaufschluss | |
DE60021714T2 (de) | Methode für die extraktion von öl durch mikroemulgierung | |
EP1704201A1 (de) | Emulgatoren für bohrspülmittel | |
WO1992022622A1 (de) | Verwendung ausgewählter oleophiler verbindungen mit erhöhter biologischer verträglichkeit zur verbesserung der ölbenetzbarkeit feinteiliger feststoffe und deren anwendung als fluid-loss-additive | |
DE19733710A1 (de) | Verfahren zur erleichterten Entsorgung von Arbeitsmitteln auf Basis von W/O-Invert-Emulsionen | |
EP0542808B1 (de) | Verwendung oberflächenaktiver estersulfonat-salze in wasser- und öl-basierten bohrspülungen und anderen bohrlochbehandlungsmitteln | |
EP0541605B1 (de) | Verwendung oberflächenaktiver alpha-sulfofettsäure-di-salze in wasser- und öl-basierten bohrspülungen und anderen bohrlochbehandlungsmitteln | |
MXPA99003997A (en) | Enhanced multicomponent mixtures for soil decomposition | |
MXPA99003998A (en) | Process for the facilitated waste disposal of working substances based on water-in-oil invert emulsions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 97199205.3 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AU AZ BR CA CN ID JP MX NO NZ RO RU SD SG TR UA US UZ VN |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 1999/00796 Country of ref document: TR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1997948769 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 1998 520005 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: PA/a/1999/003998 Country of ref document: MX |
|
ENP | Entry into the national phase |
Ref document number: 2271040 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 09297481 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1199900412 Country of ref document: VN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 69087/98 Country of ref document: AU |
|
WWP | Wipo information: published in national office |
Ref document number: 1997948769 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 335491 Country of ref document: NZ |
|
WWG | Wipo information: grant in national office |
Ref document number: 69087/98 Country of ref document: AU |
|
WWG | Wipo information: grant in national office |
Ref document number: 1997948769 Country of ref document: EP |